Nature Communications (Oct 2023)

STRA8–RB interaction is required for timely entry of meiosis in mouse female germ cells

  • Ryuki Shimada,
  • Yuzuru Kato,
  • Naoki Takeda,
  • Sayoko Fujimura,
  • Kei-ichiro Yasunaga,
  • Shingo Usuki,
  • Hitoshi Niwa,
  • Kimi Araki,
  • Kei-ichiro Ishiguro

DOI
https://doi.org/10.1038/s41467-023-42259-6
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 18

Abstract

Read online

Abstract Meiosis is differently regulated in males and females. In females, germ cells initiate meiosis within a limited time period in the fetal ovary and undergo a prolonged meiotic arrest until puberty. However, how meiosis initiation is coordinated with the cell cycle to coincide with S phase remains elusive. Here, we demonstrate that STRA8 binds to RB via the LXCXE motif. Mutation of the RB-binding site of STRA8 in female mice delays meiotic entry, which consequently delays progression of meiotic prophase and leads to precocious depletion of the oocyte pool. Single-cell RNA-sequencing analysis reveals that the STRA8–RB interaction is required for S phase entry and meiotic gene activation, ensuring precise timing of meiosis initiation in oocytes. Strikingly, the results suggest STRA8 could sequester RB from E2F during pre-meiotic G1/S transition. This study highlights the gene regulatory mechanisms underlying the female-specific mode of meiotic initiation in mice.